Canonical Allele Identifier: PA2826625317
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483888
ClinVar RCV Id: RCV000568421 RCV002528146 RCV004001068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser211Cys
CA067038
NM_001281492.2:c.632C>G